We investigate the effect of temperature on structure and dynamics of a colloidal glass created by tethering polymers to the surface of inorganic nanoparticles. Contrary to the conventional assumption, an increase in temperature slows down glassy dynamics of the material, yet causes no change in its static structure factor. We show that these findings can be explained within the soft glassy rheology framework if the noise temperature X of the glass phase is correlated with thermodynamic temperature. DOI: 10.1103/PhysRevLett.107.268302 PACS numbers: 83.80.Hj, 64.70.pv A jamming or glass transition has been observed in a wide range of soft materials including foams, emulsions, pastes, and suspensions when the fraction of the dispersed phase exceeds a critical value. Such ubiquity has led to attempts to develop a universal description of jamming, which has culminated in several phase diagrams for jammed matter [1,2]. These phase diagrams identify density, load, and temperature as the key variables that control the thermodynamics of the jamming transition, and even the physical properties of the resultant soft glassy materials. The effect of density and load on the state of jammed matter has been studied experimentally by several groups, and the findings are generally in qualitative agreement with the proposed phase diagram, typically concluding that unjamming of a glass phase occurs with decreasing density [3,4] or increasing load [5,6].In contrast, temperature, which plays a critical role in the equilibrium properties and dynamics of molecular systems, has received little systematic attention for colloidal glasses. This situation partially stems from the athermal nature of most granular systems. The common hypothesis hitherto has been that an increase in temperature will give rise to more fluidity and hence unjam the system, as proposed in previous jamming phase diagrams [1,2]. In this Letter we perform such a systematic study using self-suspended nanoparticles densely grafted with polymer chains as a model soft glassy material [7,8]. The absence of a solvent in the self-suspended nanoparticles studied here is attractive because it precludes any temperature-dependent enthalpic interactions between the solvent and the suspended phase. Our studies show that contrary to expectations, increasing temperature enhances jamming, and that subsequent lowering of the temperature unjams the system. We further show that the effect is captured on the continuum level through coupling of the so-called noise temperature X [9] emanating from co-operativity of elements in a soft glass with the thermodynamic temperature T originating from interactions of the system with its surroundings. The fundamental origin of the coupling between X and T appears to be that higher temperatures lead to greater interpenetration of polymer brushes tethered to neighboring particles.The limited utility of hard sphere colloids for exploring the physics of the glass transition and the phase space of jammed systems has been noted to result from their ...